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PMID: 670727 Published · ppublish English Comparative Study Journal Article

Studies on the microcytotoxicity test. III. Comparison of [75Se]selenomethionine with [3H]proline, Na2, 51CrO4 and [125I]iododeoxyuridine for pre-labelling target cells in long-term cytotoxicity tests.

Journal of immunological methods ·Vol. 22 ·No. 1-2 ·1978-00-00 ·Pages 23-36

Brooks CG

Abstract

Four intracellular radioisotope labels, [3H]proline, Na2 51CrO4, [75Se]selenomethionine and [125I]iododeoxyuridine, were evaluated for use in a pre-labelling long-term microcytotoxicity assay for cell-mediated immunity. Adherent rat tumour cells established in tissue culture were used as targets and the basic variables studied were labelling efficiency, toxicity and spontaneous release rates. [125I]Iododeoxyuridine was found unsuitable on account of its high toxicity and correspondingly high spontaneous release rate, and Na2 51CrO4 for its toxicity and low labelling efficiency. Of the two other radiolabels, [75Se]selenomethionine had the advantage over [3H]proline of higher labelling efficiency (especially in Ham's F10 medium), lower toxicity, and being a gamma-emitter. Furthermore, released 75Se was shown to be non-reutilisable and its retention by target cells provided an accurate measure of cell survival in an alloimmune system. Methods of calculating the results of pre-labelling cytotoxicity tests based on the total radioactivity in target cells at the beginning of the assay were found to be invalid.

MeSH Terms
Animals Chromates/metabolism Cytotoxicity Tests, Immunologic Idoxuridine/metabolism,toxicity Isotope Labeling Proline/metabolism,toxicity Rats Selenium/metabolism Selenomethionine/metabolism,toxicity Time Factors
Chemicals
Chromates Selenomethionine Proline Selenium Idoxuridine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Brooks C G
Article Info
Journal
Journal of immunological methods
Abbr.
J Immunol Methods
ISSN
0022-1759
Published
1978-00-00
Pages
23-36
Language
English
Region
Netherlands
NLM ID
1305440
Subset
IM
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